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1)  Cycloheximide [英][,saikləu'heksimaid]  [美][,saɪklo'hɛksə,maɪd, -mɪd]
环己亚胺
1.
Having treated roots with PEG and Actinomycin D or Cycloheximide,the accumulation of ABA in roots and leaves were inhibited clearly.
经放线菌素D和环己亚胺分别与PEG一起处理,根及叶片ABA增加均明显受抑制,说明此ABA增加可能来源于组织的从头生物合
2.
Methods Lycium barbarums were randomly divided into four groups:control group was 8 Lycium barbarums),Na2SeO3 group was 8 Lycium barbarums,actinomycin D(AMD) group was 16 Lycium barbarums(3 μg·L-1 AMD group and 5 μg·L-1 AMD group were respectively 8 Lycium barbarums),cycloheximide(CHM) group was 16 Lycium barbarums(0.
L-1AMD组各8株)及环己亚胺(CHM)组16株(0。
2)  cycloheximide [英][,saikləu'heksimaid]  [美][,saɪklo'hɛksə,maɪd, -mɪd]
环己酰亚胺
1.
Fermentation conditions for cycloheximide producing strain YIM41004~T;
产环己酰亚胺菌株YIM41004~T发酵条件的研究
2.
The inhibitory effect of cycloheximide on Phytophthora nicotianae of tabacoo;
环己酰亚胺对烟草疫霉菌的抑制作用
3.
Compound mutation breeding of cycloheximide-producing new strain Streptomyces yunnanensis YIM41004;
产环己酰亚胺新菌株YIM41004的复合诱变选育
3)  cycloheximide [英][,saikləu'heksimaid]  [美][,saɪklo'hɛksə,maɪd, -mɪd]
亚胺环己酮
1.
Cycloheximide(CHX), a protein synthesis inhibitor, can activate mouse eggs but the underlying mechanism is not fully known.
蛋白合成抑制剂亚胺环己酮可以诱导小鼠卵母细胞发生孤雌活化 ,但其机制尚未完全阐明。
2.
The expressions of MEPE / OF45 gene fragments were observed in the cells after cycloheximide(CHX) treatment to inhibite protein synthesis.
方法:选取人宫颈癌细胞HeLa为靶细胞,从中提取总RNA,设计扩增人MEPE/OF45基因片段的特异引物,进行RT-PCR分析;用蛋白质合成抑制剂亚胺环己酮(CHX)对细胞进行处理,观察处理前后MEPE/OF45基因的表达情况。
4)  dicyclohexylamine nitrite
亚硝酸二环己胺
1.
The physical and inhibition characteristics of dicyclohexylamine nitrite and volcanic ash tablet were determined.
测量了亚硝酸二环己胺与海泡石混合压片后的力学性能,分析了亚硝酸二环己胺与海泡石压片对金属的缓蚀性能。
2.
The preparation of dicyclohexylamine nitrite(DICHAN) and sepiolite tablet was introduced.
介绍了亚硝酸二环己胺与海泡石压片的制备工艺,并以该压片为例对气相缓蚀剂在铁制品包装中的缓蚀性能进行了研究。
5)  (-)anhydrocycloheximide
(-)脱水亚胺环己酮
6)  1,4-bis(aminocyclohexyl)methane
4,4'-亚基双环己胺
补充资料:环己亚胺
分子式:C6H11N
分子量:99.18
CAS号:111-49-9

性质:液体。沸点138℃, 相对密度0.8643,高度易燃,闪点18℃。能与水部分混溶。

制备方法:1.1,6-己二胺法1,6-己二胺经脱氨基和环化制得。2.己内酰胺法。

用途:本品是医药、农药中间体。在医药方面用于制青霉素等;在农药方面用于合成除草剂、杀菌剂;还用于橡胶硫化剂、照相药剂、防锈剂、树脂添加剂等。

说明:补充资料仅用于学习参考,请勿用于其它任何用途。
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